Related Experiment Video
Updated: Jun 3, 2026

06:09
An In Ovo Model for Testing Insulin-mimetic Compounds
Published on: April 23, 2018
Exploring the Antidiabetic Potential of Achyranthes aspera: Bioactive Compound Extraction, In vitro Efficacy, and In
Ahmed Abdulkareem Najm1,2, Zhang Yu Ming3, Ibrahim Mahmood4
1Department of Food Science, Faculty of Science and Technology, University Kebangsaan Malaysia, 43600, Bangi, Selangor, Malaysia.
Current Pharmaceutical Biotechnology
|June 2, 2026
Summary
Achyranthes aspera demonstrates potent antidiabetic effects by inhibiting key carbohydrate-digesting enzymes and enhancing glucose uptake. This traditional herb shows promise as a source of novel therapies for diabetes management.
Area of Science:
- Phytochemistry
- Pharmacology
- Computational Biology
Background:
- Diabetes mellitus incidence is rising globally, necessitating novel therapeutic strategies.
- Medicinal herbs offer a rich source of compounds with potential antidiabetic activity.
- Achyranthes aspera has traditional uses for metabolic disorders, but its mechanisms are unclear.
Purpose of the Study:
- To evaluate the antidiabetic efficacy of Achyranthes aspera using experimental and computational methods.
- To investigate its capacity to inhibit carbohydrate-digesting enzymes and enhance cellular glucose uptake.
- To elucidate the molecular mechanisms underlying its antidiabetic effects.
Main Methods:
- Aqueous leaf extract of A. aspera was analyzed for phytochemicals and antioxidant activity.
- In vitro assays assessed inhibition of α-amylase, α-glucosidase, and Dipeptidase-4 (DPP-4), cytotoxicity, and glucose uptake in L6 myotubes.
- Liquid Chromatography-Mass Spectrometry (LC-MS), molecular docking, and molecular dynamics simulations were employed.
Main Results:
- The extract showed significant phenolic and flavonoid content, correlating with antioxidant activity.
- Strong inhibition of α-amylase, α-glucosidase, and DPP-4 was observed, with some samples outperforming reference drugs.
- The extract enhanced glucose uptake in L6 myotubes without cytotoxicity, supported by computational validation of binding interactions.
Conclusions:
- Achyranthes aspera exhibits multi-target antidiabetic activity via enzyme inhibition and enhanced glucose uptake.
- Its phenolic-rich composition and validated in silico binding interactions support its therapeutic potential.
- Further in vivo studies are needed to confirm efficacy and safety for functional foods or adjunctive diabetic therapy.
Related Concept Videos
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors
α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are typically...
Acarbose and miglitol are typically...
Glucagon-like Receptor Agonists
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by the...
Dipeptidyl Peptidase 4 Inhibitors
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a significant...